HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 901954Erstellt: 25. Oktober 2026
Sodium hydride → methyl 3-chloro(N-(4-chlorobenzenesulphonyl)-N-methylaminomethyl)thiophene-2-carboxylate
https://huagongshe.com/reaction/901954
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 4-Chloro-N-methylbenzenesulfonamide | HCID 232992 | — |
| Edukt | Potassium bisulfate | HCID 516920 | — |
| Edukt | Methyl 4-(bromomethyl)-3-chlorothiophene-2-carboxylate | HCID 18376575 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | methyl 3-chloro(N-(4-chlorobenzenesulphonyl)-N-methylaminomethyl)thiophene-2-carboxylate | HCID 69208322 | 102,3% |
Reaktionsschritte
Sodium hydride (60% dispersion, 150 mg, 3.8 mmol) was added to a solution of 4-chloro-N-methylbenzenesulfonamide (640 mg, 3.1 mmol) in DMF (12 ml) while cooling in an ice/water bath. After stirring for 15 min the mixture was allowed to warm to room temperature and stirred for a further 30 min. Methyl 4-bromomethyl-3-chlorothiophene-2-carboxylate (1.08 g, 4.0 mmol) was added and the mixture was stirred for 18 h. 0.3N Potassium hydrogen sulphate solution was added and the mixture evaporated. The mixture was extracted with ethyl acetate and the organic extract was washed with brine, dried and reduced. Chromatography (25% EtOAc/75% 60-80 pet ether) yielded methyl 3-chloro(N-(4-chlorobenzenesulphonyl)-N-methylaminomethyl)thiophene-2-carboxylate (1.25 g, 79%) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07365065B2 |
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| Quelldatensatz | uspto-grants-2008_04 |
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| ORD ID | ord-337ed5aeaf244c55825edb2de5c57ca4 |
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| Quellennotiz | uspto-grants-2008_04 |
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